Canonical Allele Identifier: CA2534180402
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94974531_94974532insGTA , CM000672.2:g.94974531_94974532insGTA GRCh38
NC_000010.10:g.96734288_96734289insGTA , CM000672.1:g.96734288_96734289insGTA GRCh37
NC_000010.9:g.96724278_96724279insGTA NCBI36
NG_008385.1:g.40874_40875insGTA
NG_008385.2:g.41374_41375insGTA

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.961+2286_961+2287insGTA MANE Select ENSP00000260682.6:n.961+2286_961+2287insGTA
ENST00000643112.1:c.820-6652_820-6651insGTA ENSP00000496202.1:n.820-6652_820-6651insGTA
ENST00000260682.6:c.961+2286_961+2287insGTA ENSP00000260682.6:n.961+2286_961+2287insGTA
NM_000771.3:c.961+2286_961+2287insGTA NP_000762.2:n.961+2286_961+2287insGTA
NM_000771.4:c.961+2286_961+2287insGTA MANE Select NP_000762.2:n.961+2286_961+2287insGTA